Linked Data
ClinVar Variation Id:
498366
dbSNP Id:
rs772889861
ExAC:
X:32328283 T / C
gnomAD v2:
X-32328283-T-C
gnomAD v3:
X-32310166-T-C
gnomAD v4:
X-32310166-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32310166T>C , CM000685.2:g.32310166T>C | GRCh38 |
| NC_000023.10:g.32328283T>C , CM000685.1:g.32328283T>C | GRCh37 |
| NC_000023.9:g.32238204T>C | NCBI36 |
| NG_012232.1:g.1034444A>G , LRG_199:g.1034444A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.879A>G | ENSP00000350765.3:p.Leu293= | |
| ENST00000357033.9:c.6033A>G MANE Select | ENSP00000354923.3:p.Leu2011= | |
| ENST00000619831.5:c.2001A>G | ENSP00000479270.2:p.Leu667= | |
| ENST00000357033.8:c.6033A>G | ENSP00000354923.3:p.Leu2011= | |
| ENST00000378677.6:c.6021A>G | ENSP00000367948.2:p.Leu2007= | |
| ENST00000488902.5:n.336-93103A>G | ||
| ENST00000619831.4:c.6021A>G | ENSP00000479270.1:p.Leu2007= | |
| ENST00000620040.4:c.6033A>G | ENSP00000478150.1:p.Leu2011= | |
| NM_000109.3:c.6009A>G | NP_000100.2:p.Leu2003= | |
| NM_004006.2:c.6033A>G , LRG_199t1:c.6033A>G | NP_003997.1:p.Leu2011= | |
| NM_004009.3:c.6021A>G | NP_004000.1:p.Leu2007= | |
| NM_004010.3:c.5664A>G | NP_004001.1:p.Leu1888= | |
| NM_004011.3:c.2010A>G | NP_004002.2:p.Leu670= | |
| NM_004012.3:c.2001A>G | NP_004003.1:p.Leu667= | |
| XM_006724468.2:c.6033A>G | XP_006724531.1:p.Leu2011= | |
| XM_006724469.2:c.6009A>G | XP_006724532.1:p.Leu2003= | |
| XM_006724470.2:c.6033A>G | XP_006724533.1:p.Leu2011= | |
| XM_006724471.2:c.6033A>G | XP_006724534.1:p.Leu2011= | |
| XM_006724472.2:c.5904A>G | XP_006724535.1:p.Leu1968= | |
| XM_006724473.2:c.5895A>G | XP_006724536.1:p.Leu1965= | |
| XM_006724474.2:c.6033A>G | XP_006724537.1:p.Leu2011= | |
| XM_006724475.2:c.6033A>G | XP_006724538.1:p.Leu2011= | |
| XM_011545467.1:c.5910A>G | XP_011543769.1:p.Leu1970= | |
| XM_011545468.1:c.6033A>G | XP_011543770.1:p.Leu2011= | |
| XM_006724469.3:c.6009A>G | XP_006724532.1:p.Leu2003= | |
| XM_006724470.3:c.6033A>G | XP_006724533.1:p.Leu2011= | |
| XM_006724474.3:c.6033A>G | XP_006724537.1:p.Leu2011= | |
| XM_011545468.2:c.6033A>G | XP_011543770.1:p.Leu2011= | |
| XM_017029328.1:c.6033A>G | XP_016884817.1:p.Leu2011= | |
| XM_017029329.1:c.6033A>G | XP_016884818.1:p.Leu2011= | |
| XM_017029330.2:c.6033A>G | XP_016884819.1:p.Leu2011= | |
| XM_017029331.1:c.207A>G | XP_016884820.1:p.Leu69= | |
| NM_000109.4:c.6009A>G | NP_000100.3:p.Leu2003= | |
| NM_004006.3:c.6033A>G MANE Select | NP_003997.2:p.Leu2011= | |
| NM_004011.4:c.2010A>G | NP_004002.3:p.Leu670= | |
| NM_004012.4:c.2001A>G | NP_004003.2:p.Leu667= |